Dynamic intermediates in the radical cation diels–alder cycloaddition: lifetime and suprafacial stereoselectivity
Cation radical Diels–Alder cycloadditions proceed via an acyclic intermediate that exists on a flat region of the potential energy surface. Competition between cyclization and C–C bond rotation results in varying levels of suprafacial stereoselectivity. Quasi-classical trajectories were used to expl...
Κύριοι συγγραφείς: | Tan, J, Hirvonen, V, Paton, R |
---|---|
Μορφή: | Journal article |
Γλώσσα: | English |
Έκδοση: |
American Chemical Society
2018
|
Παρόμοια τεκμήρια
Παρόμοια τεκμήρια
-
Origins of stereoselectivity in the trans Diels-Alder paradigm.
ανά: Paton, R, κ.ά.
Έκδοση: (2010) -
Probing substituent effects in aryl-aryl interactions using stereoselective diels-alder cycloadditions
ανά: Wheeler, Steven E., κ.ά.
Έκδοση: (2012) -
Diels–Alder Cycloaddition Reactions in Sustainable Media
ανά: Maria I. L. Soares, κ.ά.
Έκδοση: (2022-02-01) -
Radical cation Diels–Alder reactions of arylidene cycloalkanes
ανά: Kaii Nakayama, κ.ά.
Έκδοση: (2022-08-01) -
Diels–Alder cycloadditions of N-arylpyrroles via aryne intermediates using diaryliodonium salts
ανά: Huangguan Chen, κ.ά.
Έκδοση: (2018-02-01)